Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate BWI76_RS07615 BWI76_RS07615 betaine-aldehyde dehydrogenase
Query= BRENDA::Q9K9B2 (515 letters) >FitnessBrowser__Koxy:BWI76_RS07615 Length = 490 Score = 252 bits (644), Expect = 2e-71 Identities = 167/489 (34%), Positives = 252/489 (51%), Gaps = 28/489 (5%) Query: 36 EYPLIINGERV--TTEDKIQSWNPARKDQLVGSVSKANQDLAEKAIQSADEAFQTWRNVN 93 E L I+G V T+ ++ NPA +++ +V A ++ ++A++SA + + W ++ Sbjct: 6 EQQLYIDGGYVSATSGKTFETINPAN-GEVLATVQAAGREDVDRAVKSAQKGQKIWAAMS 64 Query: 94 PEERANILVKAAAIIRRRKHEFSAWLVHEAGKPWKEADA-DTAEAIDFLEYYARQMIELN 152 ER+ IL KA I+R R E + + GKP E A D D LEYYA +I Sbjct: 65 AMERSRILRKAVDILRARNDELARLETLDTGKPLSETAAVDIVTGADVLEYYAG-LIPAL 123 Query: 153 RGKEILSRPGEQNRYFYT---PMGVTVTISPWNFALAIMVGTAVAPIVTGNTVVLKPAST 209 G +I P + + YT P+GV I WN+ + I + + + GN ++ KP+ Sbjct: 124 EGSQI---PLRDSSFVYTRREPLGVVAGIGAWNYPIQIALWKSAPALAAGNAMIFKPSEV 180 Query: 210 TPVVAAKFVEVLEDAGLPKGVINYVPGSGAEVGDYLVDHPKTSLITFTGSKDVGVRLYER 269 TP+ A K E+ +AGLP GV N +PG+GAE G YL +HP + I+FTG G ++ Sbjct: 181 TPLTALKLAEIYREAGLPAGVFNVLPGTGAETGQYLTEHPDIAKISFTGGVASGKKVMAN 240 Query: 270 AAVVRPGQNHLKRVIVEMGGKDTVVVDRDADLDLAAESILVSAFGFSGQKCSAGSRAVIH 329 AA + LK V +E+GGK ++V DA LDLAA+ +++ F SGQ C+ G+R + Sbjct: 241 AAA-----SSLKEVTMELGGKSPLIVCEDASLDLAADIAMMANFYSSGQVCTNGTRVFVP 295 Query: 330 KDVYDEVLEKTVALAKNLTVGDPTNRDNYMGPVIDEKAFEKIMSYIEIGKKEG-RLMTGG 388 + EK +A + GD GP++ + ++ YIE GK+EG RL+ GG Sbjct: 296 TRLKAAFEEKILARVARIRPGDLFAESTNFGPLVSFPHRDNVLRYIETGKQEGARLLCGG 355 Query: 389 EGDSSTGF----FIQPTIIADLDPEAVIMQEEIFGPVVAFSKANDFDHALEIANNTEYGL 444 E GF ++ PT+ D D + I++EEIFGPV++ +D + AL AN TEYGL Sbjct: 356 EALKGEGFDRGAWVAPTVFTDCDDQMTIVREEIFGPVMSILSYDDEEEALRRANATEYGL 415 Query: 445 TGAVIT--RNRAHIEQAKREFHVGNLYFNRNCTGAIVGYHPFGGFKMSGTDSKAGGPDYL 502 V+T NRAH + G + N G P GG+K SG + G L Sbjct: 416 AAGVVTPDLNRAH--RLIHRLEAGICWI--NTWGESPAEMPVGGYKHSGI-GRENGVQTL 470 Query: 503 ALHMQAKTV 511 + Q K++ Sbjct: 471 HSYTQIKSI 479 Lambda K H 0.316 0.134 0.388 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 563 Number of extensions: 31 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 515 Length of database: 490 Length adjustment: 34 Effective length of query: 481 Effective length of database: 456 Effective search space: 219336 Effective search space used: 219336 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory